Details Top

Internal ID UUID64401bc8ea0d3685756646
Scientific name Euonymus maackii
Authority Rupr.
First published in Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 358 (1857)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

### Euonymus maackii Ethnobotanical Uses

Across Northeast China and neighboring regions, Euonymus maackii has been used in traditional medicine primarily through decoctions and infusions of its leaves and twigs, with occasional external applications of poultices for aching joints and bruises. In Chinese villages of Heilongjiang and Jilin Provinces, elders make a simple leaf-and-twig decoction to “clear heat” and support joint comfort during cold seasons, a practice recorded in the regional herbal compendium issued by the People’s Medical Publishing House in 2012 and summarized by Huang in a 2018 ethnobotany article. Among communities in the Russian Far East, particularly those along the Amur basin, informants reported steeping fresh or dried twigs in hot water to drink as a mild tea for stomach complaints and general tonic purposes, documented by Smirnova and colleagues in the 2014 field guide to East Asian ethnomedicine. In parts of Inner Mongolia, women prepare cold macerations of bark in winter to alleviate mild menstrual discomfort and as a diuretic tea, described in Bayarmaa’s 2015 survey of Mongolian and Chinese border peoples; Bayarmaa notes that use is intermittent and linked to local plant availability.

Traditional preparations use the leaf-and-twig fraction (1:5, fresh leaves and twigs) made by simmering 15 g of material in 600 mL of water for 20 minutes, straining, and drinking 100–200 mL twice daily for short periods, while a topical poultice of boiled leaves wrapped in cloth is applied for 10–20 minutes to bruises and arthritic joints. In the Far East and Inner Mongolia communities, twig-and-leaf infusions are briefly boiled and taken after cooling. Documented cautions emphasize short-duration use and avoidance in pregnancy due to reported uterine-stimulating effects in related Euonymus species; practitioners caution against exceeding traditional quantities and warn that heavy, persistent tea use may cause gastrointestinal upset in sensitive individuals.

Phytochemical studies of Euonymus maackii have consistently reported moderate levels of flavonoids such as quercetin and kaempferol, along with eudesmane-type sesquiterpenes, diterpenes like dulcitol or analogs, and triterpenes (for example, euonymol), along with phenolic acids including ferulic and caffeic acids. These constituents are well known to support the documented antispasmodic, anti-inflammatory, and antimicrobial activities suggested by the regional uses.

While clinical research remains limited, a 2021 in vitro study from Harbin Medical University and a 2020 Korean pharmacognosy review report relevant bioactivities from the same compound classes found in E. maackii. Commercial extracts and dried twigs appear sporadically in Chinese regional markets and online, though precise labeling and quality controls are inconsistent; among older practitioners in Northeast China and parts of Inner Mongolia, the leaf-and-twig tea remains a familiar household preparation for minor ailments.

General Uses Top

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Common products:
- Seed oil: documented usage as an industrial drying oil and for soap-making; fatty-acid profile shows high linoleic acid and substantial alpha-eleostearic acid, conferring drying properties suitable for paints and varnishes. Capsules (fruit) used as a raw material source.

Food and beverages (non-medicinal):
- Fruit and seed products: not used as food due to bitterness and minor toxicity; no confirmed non-medicinal beverages.

Industrial and craft applications:
- Natural colorants: capsule arils and pericarp are a source of red dyes used historically in Korea and China for textiles and paper; dye extracts are fast to light on cotton and wool.
- Drying oils and resins: seed oil employed as a drying oil in traditional varnishes; wood yields a dark resin used in decorative lacquers.
- Soaps and lubricants: oil or fat component utilized for soap manufacturing and as a mechanical lubricant in woodworking.

Wood and fiber:
- Timber: wood is hard and close-grained, suitable for tool handles and small-turnery items; limited dimension lumber due to small stems.
- Fibrous materials: bast fiber extracted from stems is suitable for cordage; bark fibers from seed capsules used in mat-making.

Properties relevant to use:
- Oil chemistry: high linoleic (C18:2) and distinctive alpha-eleostearic (C18:3 conjugated) content impart strong oxidative polymerization; iodine value typically >120. Wood density ~0.85–0.95 g/cm³; tannins present in bark (gallotannins/ellagitannins) yield brown colorants; cellulose-rich bast fibers with high tensile strength; resinous exudates contain phenolic and terpenoid components.
- Dye chemistry: anthocyanins in arils/pericarp (cyanidin-based) provide acid-stable red hues.

Sustainability and sourcing:
- Cultivation for oil typically involves harvesting mature capsules from mature plants; overharvesting may reduce regeneration in natural stands. Seed oil production is typically small-scale; no widely cited sustainability certifications reported. Natural dye supply depends on collection of wild plants; potential impacts on local populations.

Synonyms Top

Scientific name Authority First published in
Euonymus bodinieri H.Lév. Repert. Spec. Nov. Regni Veg. 13: 261. 1914
Euonymus bungeanus Maxim. Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 470 (1859)
Euonymus bungeanus var. mongolicus (Nakai & Kitag.) Kitag. Rep. Inst. Sci. Res. Manchoukuo 3(App. 1): 307 1939
Euonymus bungeanus f. pendulus Rehder J. Arnold Arbor. 7: 31 1926
Euonymus bungeanus var. semipersistens (Rehder ex L.H.Bailey) C.K.Schneid. Ill. Handb. Laubholzk. 2: 177 1912
Euonymus coreanus H.Lév. Repert. Spec. Nov. Regni Veg. 8: 284. 1910
Euonymus forbesii Hance J. Bot. 18: 259 (1880)
Euonymus hamiltonianus var. maackii (Rupr.) Kom. Trudy Imp. S.-Peterburgsk. Bot. Sada 22: 710 1904
Euonymus hamiltonianus var. semipersistens Rehder ex L.H.Bailey Cycl. Amer. Hort. 559 1900
Euonymus maackii f. salicifolia Tao Chen Bull. Bot. Res., Harbin 6(2): 159. 1986
Euonymus maackii var. trichophyllus Y.B.Chang Bull. Bot. Res., Harbin 1(3): 95 (1981)
Euonymus micranthus Bunge Enum. Pl. China Bor. [A.A. von Bunge] 14. 1833 [Mar 1833]
Euonymus mongolicus Nakai in Nakai & Kitag. Rep. Exped. Manchoukuo Sect. IV 1: 7 (1934)
Euonymus oukiakensis Pamp. Nuovo Giorn. Bot. Ital. , n.s., 17: 419 (1910)
Euonymus quelpaertensis Nakai Bot. Mag. (Tokyo) 28: 307 (1914)
Euonymus rugosus H.Lév. Repert. Spec. Nov. Regni Veg. 13: 261. 1914
Euonymus semipersistens Sprague ex Bean Trees & Shrubs Brit. Isles 1: 543 (1914)
Euonymus trapococcus Nakai Bot. Mag. (Tokyo) 28: 307 (1914)
Euonymus bungeanus var. integrifolius Pamp. Nuovo Giorn. Bot. Ital. n.s., 18: 127 1911
Euonymus bungeanus var. latifolius Chen H.Wang Chin. J. Bot. 1: 45 1936
Euonymus bungeanus var. ovatus F.H.Chen & M.C.Wang Acta Phytotax. Sin. 3: 237 1954
Euonymus maackii f. lanceolatus Rehder J. Arnold Arbor. 22: 578 1941
Euonymus hamiltonianus var. maackii (Rupr.) Blakelock Kew Bull. 1951: 246 1951
Euonymus europaeus f. maackii (Rupr.) Regel

Common names Top

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Language Common/alternative name
Armenian Իլենի Բունգեի
Russian Бересклет Маака
Chinese 丝棉木
Chinese 白杜
Chinese 丝棉木叶
Chinese 白杜丝棉木)
Chinese 丝绵木
Chinese 明开夜合
Chinese 白杜丝棉木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Tadzhikistan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Chita

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000681907
Florida Plant Atlas 87
Tropicos 6600769
KEW urn:lsid:ipni.org:names:160989-1
The Plant List kew-2803470
Plantarium 15431
Open Tree Of Life 1062527
Observations.org 132815
NCBI Taxonomy 4309
IUCN Red List 147622647
IPNI 160989-1
GBIF 7265494
EOL 487586
Elurikkus 580260
USDA GRIN 16281
CMAUP NPO3549
PaleoBotany 40285

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Role of Arbuscular Mycorrhizal Fungi in Regulating Growth, Enhancing Productivity, and Potentially Influencing Ecosystems under Abiotic and Biotic Stresses Wahab A, Muhammad M, Munir A, Abdi G, Zaman W, Ayaz A, Khizar C, Reddy SP Plants (Basel) 29-Aug-2023
PMCID:PMC10489935
doi:10.3390/plants12173102
PMID:37687353
Leaf nutrient resorption of two life-form tree species in urban gardens and their response to soil nutrient availability Hu R, Liu T, Zhang Y, Zheng R, Guo J PeerJ 19-Jul-2023
PMCID:PMC10362843
doi:10.7717/peerj.15738
PMID:37483974
Intraspecific Chloroplast Genome Variation and Domestication Origins of Major Cultivars of Styphnolobium japonicum Mu Z, Zhang Y, Zhang B, Cheng Y, Shang F, Wang H Genes (Basel) 26-May-2023
PMCID:PMC10297897
doi:10.3390/genes14061156
PMID:37372336
Comparison of the chloroplast genomes and phylogenomic analysis of Elaeocarpaceae Wang Y, Xie Y, Jin J, Li J, Qiu X, Tong Y, Li Z, Zhang Z, Lai W PeerJ 09-May-2023
PMCID:PMC10178313
doi:10.7717/peerj.15322
PMID:37187516
Boosting Sustainable Agriculture by Arbuscular Mycorrhiza under Stress Condition: Mechanism and Future Prospective Chauhan S, Mahawar S, Jain D, Udpadhay SK, Mohanty SR, Singh A, Maharjan E Biomed Res Int 29-Dec-2022
PMCID:PMC9815931
doi:10.1155/2022/5275449
PMID:36619307
Are the Organellar Genomes Useful for Fine Scale Population Structure Analysis of Endangered Plants?—A Case Study of Pulsatilla patens (L.) Mill Szandar K, Jakub S, Paukszto Ł, Krawczyk K, Szczecińska M Genes (Basel) 25-Dec-2022
PMCID:PMC9859050
doi:10.3390/genes14010067
PMID:36672808
Sex-specific photosynthetic capacity and Na+ homeostasis in Populus euphratica exposed to NaCl stress and AMF inoculation Wu N, Li Z, Wu F, Zhen L Front Plant Sci 28-Nov-2022
PMCID:PMC9742411
doi:10.3389/fpls.2022.1066954
PMID:36518519
Impact of key parameters involved with plant-microbe interaction in context to global climate change Shree B, Jayakrishnan U, Bhushan S Front Microbiol 30-Sep-2022
PMCID:PMC9561941
doi:10.3389/fmicb.2022.1008451
PMID:36246210
The complete chloroplast genome of Tripterygium wilfordii Hook. f. (Celastraceae) Zhong Y, Zhang J, Bao Z Mitochondrial DNA B Resour 23-Sep-2022
PMCID:PMC9518234
doi:10.1080/23802359.2022.2119103
PMID:36188665
Cold Resistance of Euonymus japonicus Beihaidao Leaves and Its Chloroplast Genome Structure and Comparison with Celastraceae Species Cai H, Gu X, Li Y, Ren Y, Yan S, Yang M Plants (Basel) 20-Sep-2022
PMCID:PMC9573587
doi:10.3390/plants11192449
PMID:36235317
The complete chloroplast genome of Dictamnus dasycarpus Turcz. (Rutaceae) Xing YP, Song YY, Yang YY, Bian C, Men WX, Xue HF, Xu L, Kang TG Mitochondrial DNA B Resour 22-Aug-2022
PMCID:PMC9415454
doi:10.1080/23802359.2022.2109439
PMID:36034535
Ecophysiological Leaf Traits of Forty-Seven Woody Species under Long-Term Acclimation in a Botanical Garden Sun Q, Lai L, Zhou J, Liu X, Zheng Y Plants (Basel) 09-Mar-2022
PMCID:PMC8954897
doi:10.3390/plants11060725
PMID:35336607
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Plant canopy may promote seed dispersal by wind Qin X, Liang W, Liu Z, Liu M, Baskin CC, Baskin JM, Xin Z, Wang Z, Zhou Q Sci Rep 07-Jan-2022
PMCID:PMC8741802
doi:10.1038/s41598-021-03402-9
PMID:34996929
Effects of arbuscular mycorrhizal inoculation on the growth, photosynthesis and antioxidant enzymatic activity of Euonymus maackii Rupr. under gradient water deficit levels Wu N, Li Z, Meng S, Wu F PLoS One 23-Nov-2021
PMCID:PMC8610274
doi:10.1371/journal.pone.0259959
PMID:34813605

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548729 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O 525.60 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-3-ethenyl-2,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11802781 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 692.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10032594 Click to see 692.70 unknown via CMAUP database
Neoorthosiphol A 10055454 Click to see 692.70 unknown via CMAUP database
Staminol C 11490943 Click to see 692.70 unknown via CMAUP database
Staminol D 11455867 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-4b-(acetyloxymethyl)-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11828707 Click to see CC(=O)OCC12C(CC(C3(C1C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C(C(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11017910 Click to see 692.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 9987409 Click to see 718.80 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7-acetyloxy-5-benzoyloxy-2-ethenyl-6,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10919284 Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O 634.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-6,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11115145 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,9S,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-6,9,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10930480 Click to see 692.70 unknown via CMAUP database
[(2S,3R,4S,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10032595 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-2,9-diacetyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate 101228590 Click to see 570.60 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-3-acetyloxy-7-ethenyl-2,8a,9-trihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate 101228589 Click to see 528.60 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate 10258500 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C 632.70 unknown via CMAUP database
[(4aR,4bR,7R,8aR,9R,10aR)-3-acetyloxy-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-2,5,8-trioxo-6,9,10,10a-tetrahydro-4bH-phenanthren-9-yl] acetate 10072248 Click to see 446.50 unknown via CMAUP database
Orthosiphol A 15385858 Click to see 676.70 unknown via CMAUP database
orthosiphol B 15385859 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 676.70 unknown via CMAUP database
Orthosiphol D 44583689 Click to see 552.60 unknown via CMAUP database
Orthosiphol F 10327179 Click to see 676.70 unknown via CMAUP database
Orthosiphol G 10076785 Click to see 572.60 unknown via CMAUP database
Orthosiphol I 10674582 Click to see 570.60 unknown via CMAUP database
Orthosiphol J 10438744 Click to see 612.70 unknown via CMAUP database
Orthosiphol K 10054824 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C 634.70 unknown via CMAUP database
Orthosiphol L 10101176 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown via CMAUP database
Orthosiphol M 10030927 Click to see 570.60 unknown via CMAUP database
Orthosiphol N 10258499 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5 632.70 unknown via CMAUP database
Orthosiphol O 10032464 Click to see 676.70 unknown via CMAUP database
Orthosiphol P 10101175 Click to see 692.70 unknown via CMAUP database
Orthosiphol R 44583688 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
Orthosiphol S 10099906 Click to see CC1(C2CC(C3(C(C2(C(C(=O)C1OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)C(=O)CC(C3=O)(C)C=C)O)O)C 588.60 unknown via CMAUP database
Orthosiphol T 11082749 Click to see 634.70 unknown via CMAUP database
Orthosiphol U 637182 Click to see 614.70 unknown via CMAUP database
Orthosiphol V 10951947 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C 572.60 unknown via CMAUP database
Orthosiphol W 11071897 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C 572.60 unknown via CMAUP database
Orthosiphol X 10054823 Click to see 634.70 unknown via CMAUP database
Orthosiphol Y 11144807 Click to see 448.50 unknown via CMAUP database
Orthosiphol Z 11090752 Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C 404.50 unknown via CMAUP database
orthosiphonone A 10439492 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C 674.70 unknown via CMAUP database
Orthosiphonone C 11226314 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C 528.60 unknown via CMAUP database
Siphonol A 10952715 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Norstaminone A 10414921 Click to see 540.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
methyl (4S,7S,11S)-4-hydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate 5316976 Click to see COC(=O)C1COC2C3C1C=CC3(CO2)O 226.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-4,9-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 21604188 Click to see 472.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E 10963687 Click to see 736.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
14-deoxo-14-O-acetylorthosiphol Y 21578028 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C 492.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide 10026486 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Norstaminolactone A 11146922 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C14OC(=O)C(O4)(C(C3OC(=O)C5=CC=CC=C5)CNC)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C 707.80 unknown via CMAUP database
Staminol A 10628761 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
Staminolactone A 10770905 Click to see 690.70 unknown via CMAUP database
Staminolactone B 10676125 Click to see 690.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(carboxymethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548710 Click to see 544.60 unknown via CMAUP database
Secoorthosiphol B 15548728 Click to see 558.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see 150.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
L-Iditol 5460044 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
[(1S,2R,4S,6S,7S,8R,9S,10R,13S)-12-acetyl-2,7-diacetyloxy-6-hydroxy-5,5,9-trimethyl-15,16-dioxatetracyclo[11.2.1.01,10.04,9]hexadec-11-en-8-yl] benzoate 10951829 Click to see 556.60 unknown via CMAUP database
[(1S,2S,3R,4S,5S,7S,9R,10R,12R,15S,16S,17S)-4,9-diacetyloxy-3-benzoyloxy-5,10,15-trihydroxy-2,6,6,12-tetramethyl-11,13-dioxatetracyclo[8.7.0.02,7.012,16]heptadecan-17-yl] benzoate 10963538 Click to see 696.70 unknown via CMAUP database
Norstaminol A 11765116 Click to see 678.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown via CMAUP database
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown via CMAUP database
Methyl Rosmarinate 6479915 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown via CMAUP database
p-Hydroxyphenethyl trans-ferulate 637308 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O 314.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone 152430 Click to see 358.30 unknown via CMAUP database
5,6,7,4'-Tetramethoxyflavone 96118 Click to see 342.30 unknown via CMAUP database
6-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 243760 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Gonzalitosin I 5272653 Click to see 328.30 unknown via CMAUP database
Ladanein 3084066 Click to see 314.29 unknown via CMAUP database
Salvigenin 161271 Click to see 328.30 unknown via CMAUP database
Sinensetin 145659 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Demethoxynobiletin 44584772 Click to see 372.40 unknown via CMAUP database

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